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Increased Plasma Chemokine Levels in Children with Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is caused by loss of paternally expressed genes from the 15q11-q13 region and reportedly rearranged as a cause of autism. Additionally, increased inflammatory markers and features of autism are reported in PWS. Cytokines encoded by genes involved with inflammation, cell p...
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| Publicado en: | Am J Med Genet A |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2015
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6686673/ https://ncbi.nlm.nih.gov/pubmed/25691409 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.36908 |
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